CN106117018A - The method of phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery - Google Patents

The method of phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery Download PDF

Info

Publication number
CN106117018A
CN106117018A CN201610520456.XA CN201610520456A CN106117018A CN 106117018 A CN106117018 A CN 106117018A CN 201610520456 A CN201610520456 A CN 201610520456A CN 106117018 A CN106117018 A CN 106117018A
Authority
CN
China
Prior art keywords
level concentration
phenol
isopropylbenzene
gauge pressure
operation temperature
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN201610520456.XA
Other languages
Chinese (zh)
Other versions
CN106117018B (en
Inventor
杨军
顾静苒
李真泽
张斌
何琨
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sinopec Engineering Group Co Ltd
Sinopec Shanghai Engineering Co Ltd
Original Assignee
Sinopec Engineering Group Co Ltd
Sinopec Shanghai Engineering Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sinopec Engineering Group Co Ltd, Sinopec Shanghai Engineering Co Ltd filed Critical Sinopec Engineering Group Co Ltd
Priority to CN201610520456.XA priority Critical patent/CN106117018B/en
Publication of CN106117018A publication Critical patent/CN106117018A/en
Application granted granted Critical
Publication of CN106117018B publication Critical patent/CN106117018B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C37/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring
    • C07C37/08Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom of a six-membered aromatic ring by decomposition of hydroperoxides, e.g. cumene hydroperoxide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C407/00Preparation of peroxy compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • C07C45/51Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
    • C07C45/53Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition of hydroperoxides
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/10Process efficiency
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

Abstract

A kind of method that the present invention relates to phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, mainly solves the problem that in prior art, energy consumption is higher.The present invention is by a kind of method using phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, oxidation reactor charging and one-level concentration tower is used to eject material technological means of heat exchange in the heat exchanger of one-level concentration tower top, reach to reduce low low-pressure steam 0.21 kg/kg phenol, reduce the technical purpose of cooling water 11.0 kg/kg phenol, and nominal situation can be suitable for, driving operating mode, the technical scheme of operating mode of stopping in emergency different condition operation running preferably solves the problems referred to above, can be used in phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery.

Description

The method of phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery
Technical field
A kind of method that the present invention relates to phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery.
Background technology
Phenol is the colourless acicular crystal with special odor, is a kind of multiduty Chemical Manufacture raw material.Acetone is one Plant the chemical solvent of common highly volatile.Number of patent application US20110301384A1 cumene oxidation system and patent Shen Please the manufacture method of number CN200580006398.9 cumene hydroperoxide, describe and carry out isopropylbenzene with dry method and contain in a wet process Carrier of oxygen carries out oxidation reaction, the technique preparing cumyl hydroperoxide.Number of patent application CN201410719776.9 reduces benzene The method of phenol acetone device oxidation reaction unit energy consumption, disclose oxidation charging cumene stream by oxidizing tower heat exchanger with Reflux stream heat exchange at the bottom of oxidizing tower, further enters oxidizing tower and reacts after preheating, reach to recycle heat of reaction, have Effect reduces the method for energy consumption purpose.Number of patent application CN201410719763.1 phenol-acetone device oxidation reaction unit reduces energy The method of consumption, discloses oxidation charging cumene stream and successively passes through 2# oxidizing tower heat exchanger and 1# oxidizing tower heat exchanger, Respectively with 2# and 1# oxidizing tower at the bottom of reflux stream heat exchange, further preheating after enter oxidizing tower react, reach reclaim profit Method by heat of reaction, effectively reduction energy consumption purpose.The method of patent No. WO2014153040A2 acetone and phenol with System, a kind of method describing acetone and phenol, during crude acetone column acetone and phenol, use crude acetone Top gaseous phase pre-thermal oxide charging isopropylbenzene reaches the purpose of Appropriate application heat energy.
Prior art generates cumyl hydroperoxide at isopropylbenzene dry process reaction, during preparing phenol-acetone, at oxygen Changing unit and arrange an oxidation feed preheater, the isopropylbenzene charging of oxidizing tower is preheated to most preferably feed temperature with low low-pressure steam Degree.Meanwhile, at cumyl hydroperoxide concentration unit, one-level concentration tower top gas phase discharging cooling water section is condensed into liquid Phase, liquid-phase reflux feeds workshop section's isopropylbenzene alkaline bath to oxidation, and gas phase enters concentration tail gas cryoprobe and condenses further.Oxidizing tower Feeding preheating needs to consume a large amount of low low-pressure steam, and the condensation of one-level concentration top gaseous phase then needs to consume and cools down water in a large number, deposits Big at utility consumption, the problems such as Energy harvesting is unreasonable.
Summary of the invention
The technical problem to be solved is the problem that in prior art, energy consumption is higher, it is provided that a kind of new phenol third The method of ketone device cumyl hydroperoxide upgrading system waste heat recovery.The method has the advantage that energy consumption is relatively low.
For solving the problems referred to above, the technical solution used in the present invention is as follows: a kind of phenol-acetone device hydrogen peroxide isopropyl The method of benzene upgrading system waste heat recovery, isopropylbenzene material (2) is by one-level concentration tower top heat exchanger (22) and one-level concentration tower Top gas light component (6) mutually carries out heat exchange, and the isopropylbenzene material (4) after heating is preheated to charging by oxidation feed preheater (21) Entering the air material (15) being passed through in oxidation reactor (25), with reactor after temperature occurs oxidation reaction to generate hydrogen peroxide Isopropylbenzene (16), the oxidized tail gas (17) generated in oxidation reactor (25) send oxidized tail gas condenser;Fresh isopropylbenzene (18) Carrying out material rectification with the material (19) entrance one-level concentration tower (26) carrying out autoxidation blow tank to separate, tower reactor heavy constituent (20) is sent Two grades of concentration towers, the light component of one-level concentration top gaseous phase (6) first in one-level concentration tower top heat exchanger (22) with isopropylbenzene thing Material (2) heat exchange, then one-level concentration overhead condenser (23) the continuation condensation through series connection, uncooled gaseous phase materials (8) enters Concentration tail gas cryoprobe (24) condenses further, and in concentration tail gas cryoprobe (24), to deliver to concentration true for uncooled fixed gas (9) Empty spraying system;The condensed fluid (12) formed in one-level concentration overhead condenser (23) and concentration tail gas cryoprobe (24) are formed Condensed fluid (13) merge into material (14) and remove isopropylbenzene alkaline bath;During nominal situation, one-level concentration tower top heat exchanger (22) is cold The valve (10) of side parallel connection by-pass line is the normally off, and the valve (11) of hot side parallel connection by-pass line is the normally off, oxidation reaction charging isopropyl Benzene material (2) and the light component of one-level concentration top gaseous phase (6) carry out heat exchange;During driving operating mode, open bypass valve (10), isopropyl Benzene material (2) flows through from this bypass valve (10), and oxidation charging isopropylbenzene (4) carries out pre-by oxidation feed preheater (21) Heat;During operating mode of stopping in emergency, opening bypass valve (11), the light component of one-level concentration top gaseous phase (6) is from this bypass valve (11) Flowing through, one-level concentration top gaseous phase (7) condenses through one-level concentration overhead condenser (23), enters back into concentration tail gas cryoprobe (24) condense further.
In technique scheme, it is preferable that heat exchanger (22) hot side, one-level concentration tower top operation temperature is 60~100 DEG C; Operation gauge pressure is 0.005~0.020MPa;Cold side operation temperature is 30~90 DEG C;Operation gauge pressure is 0.3~1.5MPa;One-level carries Dense overhead condenser hot side operation temperature is 40~80 DEG C;Operation gauge pressure is 0.005~0.020MPa;Oxidation feed preheater (21) operation temperature in cold side is 30~110 DEG C;Operation gauge pressure is 0.3~1.5MPa.
In technique scheme, it is highly preferred that heat exchanger (22) hot side, one-level concentration tower top operation temperature is 65~95 DEG C; Operation gauge pressure is 0.008~0.018MPa;Cold side operation temperature is 35~85 DEG C;Operation gauge pressure is 0.5~1.2MPa;One-level carries Dense overhead condenser (23) hot side operation temperature is 45~75 DEG C;Operation gauge pressure is 0.008~0.018MPa;Oxidation feeding preheating Device (21) cold side operation temperature is 40~105 DEG C;Operation gauge pressure is 0.5~1.2MPa.
In technique scheme, most preferably, operation temperature in one-level concentration tower top heat exchanger (22) hot side is 70~90 DEG C; Operation gauge pressure is 0.010~0.015MPa;Cold side operation temperature is 40~80 DEG C;Operation gauge pressure is 0.6~1.0MPa;One-level carries Dense overhead condenser (23) hot side operation temperature is 50~70 DEG C;Operation gauge pressure is 0.010~0.015MPa;Oxidation feeding preheating Device (21) cold side operation temperature is 50~100 DEG C;Operation gauge pressure is 0.6~1.0MPa.
In technique scheme, it is preferable that oxidation feed preheater (21) uses low low-pressure steam to preheat;One-level concentration tower Cooling water condensation is used on top condenser (23);Concentration tail gas cryoprobe (24) condenses with chilled water.
In technique scheme, it is preferable that the reaction condition of oxidation reactor (25): operation temperature is 80~110 DEG C, behaviour It is 0.2~0.4MPa as gauge pressure;The mass ratio that isopropylbenzene (5) charging and compressed air (15) feed is: isopropylbenzene: air=10 ~20:1;Isopropylbenzene conversion per pass is 3.2~8.5%.
In technique scheme, it is preferable that isopropylbenzene (5) feeding temperature is 80~110 DEG C.
In technique scheme, it is preferable that the operating condition of one-level concentration tower (26): operation temperature is 90~170 DEG C, behaviour It is 0.015~0.035MPa as gauge pressure.
In technique scheme, it is preferable that the operating condition of concentration tail gas cryoprobe (24): operation temperature is 20~50 DEG C, operation absolute pressure is 0.010~0.020MPa.
The isopropylbenzene that oxidation reactor is fed by the present invention heats in the heat exchanger of one-level concentration tower top, enter back into aoxidize into Material preheater utilizes low low-pressure steam to continue to be preheated to optimal feeding temperature;One-level concentration top gaseous phase is also at one-level concentration simultaneously Tower top heat exchanger condenses, then utilizes cooling water to continue condensation through one-level concentration overhead condenser;One-level concentration tower takes one's place heat Device heat exchange amount is 112.3 kcal/kg phenol.Thus can reduce low low-pressure steam and consume 0.21 kg/kg phenol, reduce Cooling-water consumption 11.0 kg/kg phenol, and the present invention can be suitable for nominal situation, operating mode of driving, operating mode of stopping in emergency Etc. the operation running of different condition, achieve preferable technique effect.
Accompanying drawing explanation
Fig. 1 is the schematic flow sheet of the method for the invention.
In Fig. 1,1, oxidation reaction charging;2, isopropylbenzene material;3, the isopropylbenzene after the heat exchanger heat exchange of one-level concentration tower top Material;4, through the isopropylbenzene material of bypass valve 10;5, the isopropylbenzene material after the preheating of oxidation feed preheater;6, one-level carries The light component of dense top gaseous phase;7, one-level concentration tower top condenser inlet material;8, one-level concentration tower top condensator outlet gas gas-phase objects Material;9, fixed gas;10, valve;11, valve;12, one-level concentration tower top condensator outlet condensed fluid;13, concentration tail gas cryoprobe Condensed fluid;14, the material of isopropylbenzene alkaline bath is removed;15, air material;16, cumyl hydroperoxide;17, oxidized tail gas; 18, fresh isopropylbenzene;19, the material of autoxidation blow tank is carried out;20, one-level concentration tower reactor heavy constituent;21, oxidation feeding preheating Device;22, one-level concentration tower top heat exchanger;23, one-level concentration overhead condenser;24, concentration tail gas cryoprobe;25, oxidation reaction Device;26, one-level concentration tower.
Below by embodiment, the invention will be further elaborated, but is not limited only to the present embodiment.
Detailed description of the invention
[embodiment 1]
A kind of method of phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, as it is shown in figure 1, isopropylbenzene Material (2) carries out heat exchange, after heating by one-level concentration tower top heat exchanger (22) and the light component of one-level concentration top gaseous phase (6) Isopropylbenzene material (4) enters oxidation reactor (25), with reaction after being preheated to feeding temperature by oxidation feed preheater (21) The air material (15) being passed through in device occurs oxidation reaction to generate generation in cumyl hydroperoxide (16), oxidation reactor (25) Oxidized tail gas (17) send oxidized tail gas condenser;Fresh isopropylbenzene (18) and come autoxidation blow tank material (19) enter one Level concentration tower (26) carries out material rectification separation, and tower reactor heavy constituent (20) send two grades of concentration towers, light group of one-level concentration top gaseous phase Point (6) first in one-level concentration tower top heat exchanger (22) with isopropylbenzene material (2) heat exchange, then the one-level concentration tower top through series connection Condenser (23) continues condensation, and uncooled gaseous phase materials (8) enters concentration tail gas cryoprobe (24) and condenses further, concentration tail In gas cryoprobe (24), uncooled fixed gas (9) delivers to concentration airless injection system;In one-level concentration overhead condenser (23) The condensed fluid (13) formed in the condensed fluid (12) formed and concentration tail gas cryoprobe (24) is merged into material (14) and is removed isopropylbenzene Alkaline bath;During nominal situation, the valve (10) of one-level concentration tower top heat exchanger (22) cold side parallel connection by-pass line is the normally off, and hot side is also The valve (11) of connection by-pass line is the normally off, oxidation reaction charging isopropylbenzene material (2) and the light component of one-level concentration top gaseous phase (6) Carry out heat exchange;During driving operating mode, opening bypass valve (10), isopropylbenzene material (2) flows through from this bypass valve (10), aoxidize into Material isopropylbenzene (4) is preheated by oxidation feed preheater (21);During operating mode of stopping in emergency, open bypass valve (11), one The level light component of concentration top gaseous phase (6) flows through from this bypass valve (11), and one-level concentration top gaseous phase (7) is through one-level concentration tower Top condenser (23) condensation, enters back into concentration tail gas cryoprobe (24) and condenses further.
The production scale of phenol-acetone device is 100,000 tons/year, uses the cumyl hydroperoxide upgrading system of the present invention The method of waste heat recovery, process operation parameter is: newly-increased exchanger heat side, one-level concentration tower top operation temperature is 75 DEG C, operation Pressure (gauge pressure) is 0.010MPa;Cold side operation temperature is 30 DEG C, and operation pressure (gauge pressure) is 0.9MPa.One-level concentration tower top is cold Condenser hot side operation temperature is 45 DEG C, and operation pressure (gauge pressure) is 0.010MPa.Operation temperature in oxidation feed preheater cold side is 50 DEG C, operation pressure (gauge pressure) is 0.9MPa.Oxidation reactor operation temperature is 102 DEG C, and operation pressure (gauge pressure) is 0.32MPa;Isopropylbenzene charging is isopropylbenzene with the mass ratio of compressed air charging: air=16.5:1;Isopropylbenzene conversion per pass Rate is 5.5%.Isopropylbenzene feeding temperature is 102 DEG C.One-level concentration tower tower top operation temperature is 95 DEG C, and tower reactor operation temperature is 155 DEG C, operation pressure (gauge pressure) is 0.028MPa.Concentration tail gas cryoprobe operation temperature is 30 DEG C, and operation pressure (absolute pressure) is 0.013MPa.Thus, reduce low low-pressure steam consume 1.64 ton hour and reduce cooling-water consumption 86.0 ton hour.
[embodiment 2]
According to the condition described in embodiment 1 and step, simply phenol-acetone production scale changes 200,000 tons/year into.Use this The method of the cumyl hydroperoxide upgrading system waste heat recovery of invention, process operation parameter is: newly-increased one-level concentration tower top Exchanger heat side operation temperature is 95 DEG C, and operation pressure (gauge pressure) is 0.010MPa;Cold side operation temperature is 50 DEG C, operates pressure (gauge pressure) is 0.9MPa.One-level concentration overhead condenser hot side operation temperature is 75 DEG C, and operation pressure (gauge pressure) is 0.010MPa. Operation temperature in oxidation feed preheater cold side is 105 DEG C, and operation pressure (gauge pressure) is 0.9MPa.Oxidation reactor operation temperature is 105 DEG C, operation pressure (gauge pressure) is 0.35MPa;Isopropylbenzene charging is isopropylbenzene with the mass ratio of compressed air charging: air= 18.2:1;Isopropylbenzene conversion per pass is 5.9%.Isopropylbenzene feeding temperature is 105 DEG C.One-level concentration tower tower top operation temperature is 101 DEG C, tower reactor operation temperature is 163 DEG C, and operation pressure (gauge pressure) is 0.032MPa.Concentration tail gas cryoprobe operation temperature is 42 DEG C, operation pressure (absolute pressure) is 0.017MPa.Thus, reduce low low-pressure steam consume 3.28 ton hour and reduce cooling water disappear Consume 171.9 ton hour.
[embodiment 3]
According to the condition described in embodiment 1 and step, simply phenol-acetone production scale changes 350,000 tons/year into.Use this The method of the cumyl hydroperoxide upgrading system waste heat recovery of invention, process operation parameter is: newly-increased one-level concentration tower top Exchanger heat side operation temperature is 85 DEG C, and operation pressure (gauge pressure) is 0.010MPa;Cold side operation temperature is 40 DEG C, operates pressure (gauge pressure) is 0.9MPa.One-level concentration overhead condenser hot side operation temperature is 55 DEG C, and operation pressure (gauge pressure) is 0.010MPa. Operation temperature in oxidation feed preheater cold side is 75 DEG C, and operation pressure (gauge pressure) is 0.9MPa.Oxidation reactor operation temperature is 107 DEG C, operation pressure (gauge pressure) is 0.37MPa;Isopropylbenzene charging is isopropylbenzene with the mass ratio of compressed air charging: air= 17.9:1;Isopropylbenzene conversion per pass is 7.0%.Isopropylbenzene feeding temperature is 107 DEG C.One-level concentration tower tower top operation temperature is 109 DEG C, tower reactor operation temperature is 166 DEG C, and operation pressure (gauge pressure) is 0.033MPa.Concentration tail gas cryoprobe operation temperature is 46 DEG C, operation pressure (absolute pressure) is 0.019MPa.Thus, reduce low low-pressure steam consume 5.74 ton hour and reduce cooling water disappear Consume 300.8 ton hour.
[embodiment 4]
According to the condition described in embodiment 1 and step, simply phenol-acetone production scale changes 400,000 tons/year into.Use this The method of the cumyl hydroperoxide upgrading system waste heat recovery of invention, process operation parameter is: newly-increased one-level concentration tower top Exchanger heat side operation temperature is 80 DEG C, and operation pressure (gauge pressure) is 0.010MPa;Cold side operation temperature is 40 DEG C, operates pressure (gauge pressure) is 0.9MPa.One-level concentration overhead condenser hot side operation temperature is 50 DEG C, and operation pressure (gauge pressure) is 0.010MPa. Operation temperature in oxidation feed preheater cold side is 68 DEG C, and operation pressure (gauge pressure) is 0.9MPa.Oxidation reactor operation temperature is 93 DEG C, operation pressure (gauge pressure) is 0.25MPa;Isopropylbenzene charging is isopropylbenzene with the mass ratio of compressed air charging: air= 13.2:1;Isopropylbenzene conversion per pass is 4.1%.Isopropylbenzene feeding temperature is 93 DEG C.One-level concentration tower tower top operation temperature is 91 DEG C, tower reactor operation temperature is 153 DEG C, and operation pressure (gauge pressure) is 0.016MPa.Concentration tail gas cryoprobe operation temperature is 22 DEG C, operation pressure (absolute pressure) is 0.011MPa.Thus, reduce low low-pressure steam consume 6.56 ton hour and reduce cooling water disappear Consume 343.8 ton hour.
[embodiment 5]
According to the condition described in embodiment 4 and step, phenol-acetone production scale is 400,000 tons/year, simply technological operation Parameter change.The method using the cumyl hydroperoxide upgrading system waste heat recovery of the present invention, process operation parameter is: newly-increased Exchanger heat side, one-level concentration tower top operation temperature be 60 DEG C, operation pressure (gauge pressure) be 0.005MPa;Cold side operation temperature Being 30 DEG C, operation pressure (gauge pressure) is 0.3MPa.One-level concentration overhead condenser hot side operation temperature is 40 DEG C, operates pressure (gauge pressure) is 0.005MPa.Operation temperature in oxidation feed preheater cold side is 30 DEG C, and operation pressure (gauge pressure) is 0.3MPa.Oxidation Reactor operation temperature is 80 DEG C, and operation pressure (gauge pressure) is 0.2MPa;The mass ratio that isopropylbenzene charging feeds with compressed air For isopropylbenzene: air=10:1;Isopropylbenzene conversion per pass is 3.2%.Isopropylbenzene feeding temperature is 80 DEG C.One-level concentration tower tower Top operation temperature is 90 DEG C, and tower reactor operation temperature is 150 DEG C, and operation pressure (gauge pressure) is 0.015MPa.Concentration tail gas cryoprobe Operation temperature is 20 DEG C, and operation pressure (absolute pressure) is 0.010MPa.Thus, reduce low low-pressure steam and consume 6.49 ton hour also Reduce cooling-water consumption 347.2 ton hour.
[embodiment 6]
According to the condition described in embodiment 4 and step, phenol-acetone production scale is 400,000 tons/year, simply technological operation Parameter change.The method using the cumyl hydroperoxide upgrading system waste heat recovery of the present invention, process operation parameter is: newly-increased Exchanger heat side, one-level concentration tower top operation temperature be 100 DEG C, operation pressure (gauge pressure) be 0.020MPa;Cold side operation temperature Being 90 DEG C, operation pressure (gauge pressure) is 1.5MPa.One-level concentration overhead condenser hot side operation temperature is 80 DEG C, operates pressure (gauge pressure) is 0.020MPa.Operation temperature in oxidation feed preheater cold side is 110 DEG C, and operation pressure (gauge pressure) is 1.5MPa.Oxygen Changing reactor operation temperature is 110 DEG C, and operation pressure (gauge pressure) is 0.4MPa;The quality that isopropylbenzene charging feeds with compressed air Ratio is isopropylbenzene: air=20:1;Isopropylbenzene conversion per pass is 8.5%.Isopropylbenzene feeding temperature is 110 DEG C.One-level concentration Column overhead operation temperature is 110 DEG C, and tower reactor operation temperature is 170 DEG C, and operation pressure (gauge pressure) is 0.035MPa.Concentration tail gas is cold Freezing device operation temperature is 50 DEG C, and operation pressure (absolute pressure) is 0.020MPa.Thus, reduce low low-pressure steam consume 6.63 tons/little Time and reduce cooling-water consumption 339.7 ton hour.
Obviously, the method using the present invention, mainly solve oxidation reactor feeding preheating and one-level concentration in prior art Top gaseous phase condensation uses low low-pressure steam and cooling water respectively, there is public work and consumes the problems such as big, uses oxidation reaction Device charging and one-level concentration tower eject material technological means of heat exchange in the heat exchanger of one-level concentration tower top, reach to reduce low pressure and steam Vapour 0.21 kg/kg phenol, reduces the technical purpose of cooling water 11.0 kg/kg phenol, and the present invention can be suitable for Nominal situation, operating mode of driving, the operation running of the different conditions such as operating mode of stopping in emergency, preferably solve this problem, can It is applied to prepare in the commercial production of phenol-acetone.

Claims (9)

1. a method for phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, isopropylbenzene material (2) passes through One-level concentration tower top heat exchanger (22) and the light component of one-level concentration top gaseous phase (6) carry out heat exchange, the isopropylbenzene material after heating (4) it is passed through in entrance oxidation reactor (25), with reactor after being preheated to feeding temperature by oxidation feed preheater (21) Air material (15) occurs oxidation reaction to generate the oxidized tail gas generated in cumyl hydroperoxide (16), oxidation reactor (25) (17) oxidized tail gas condenser is sent;Fresh isopropylbenzene (18) and come autoxidation blow tank material (19) enter one-level concentration tower (26) carrying out material rectification separation, tower reactor heavy constituent (20) send two grades of concentration towers, and the light component of one-level concentration top gaseous phase (6) first exists With isopropylbenzene material (2) heat exchange in one-level concentration tower top heat exchanger (22), then the one-level concentration overhead condenser through series connection (23) continuing condensation, uncooled gaseous phase materials (8) enters concentration tail gas cryoprobe (24) and condenses further, and concentration tail gas is freezing In device (24), uncooled fixed gas (9) delivers to concentration airless injection system;One-level concentration overhead condenser (23) is formed The condensed fluid (13) formed in condensed fluid (12) and concentration tail gas cryoprobe (24) is merged into material (14) and is removed isopropylbenzene alkaline bath; During nominal situation, the valve (10) of one-level concentration tower top heat exchanger (22) cold side parallel connection by-pass line is the normally off, and the parallel connection of hot side bypasses The valve (11) of pipeline is the normally off, and oxidation reaction charging isopropylbenzene material (2) is changed with the light component of one-level concentration top gaseous phase (6) Heat;During driving operating mode, opening bypass valve (10), isopropylbenzene material (2) flows through from this bypass valve (10), oxidation charging isopropyl Benzene (4) is preheated by oxidation feed preheater (21);During operating mode of stopping in emergency, open bypass valve (11), one-level concentration The light component of top gaseous phase (6) flows through from this bypass valve (11), and one-level concentration top gaseous phase (7) is through one-level concentration overhead condensation Device (23) condenses, and enters back into concentration tail gas cryoprobe (24) and condenses further.
The most according to claim 1, the method for phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, it is special Levy and be that heat exchanger (22) hot side, one-level concentration tower top operation temperature is 60~100 DEG C;Operation gauge pressure be 0.005~ 0.020MPa;Cold side operation temperature is 30~90 DEG C;Operation gauge pressure is 0.3~1.5MPa;The hot side of one-level concentration overhead condenser Operation temperature is 40~80 DEG C;Operation gauge pressure is 0.005~0.020MPa;Operation temperature in oxidation feed preheater (21) cold side is 30~110 DEG C;Operation gauge pressure is 0.3~1.5MPa.
The most according to claim 2, the method for phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, it is special Levy and be that heat exchanger (22) hot side, one-level concentration tower top operation temperature is 65~95 DEG C;Operation gauge pressure is 0.008~0.018MPa; Cold side operation temperature is 35~85 DEG C;Operation gauge pressure is 0.5~1.2MPa;One-level concentration overhead condenser (23) hot side operation temperature Degree is 45~75 DEG C;Operation gauge pressure is 0.008~0.018MPa;Oxidation feed preheater (21) cold side operation temperature be 40~ 105℃;Operation gauge pressure is 0.5~1.2MPa.
The most according to claim 3, the method for phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, it is special Levy and be that heat exchanger (22) hot side, one-level concentration tower top operation temperature is 70~90 DEG C;Operation gauge pressure is 0.010~0.015MPa; Cold side operation temperature is 40~80 DEG C;Operation gauge pressure is 0.6~1.0MPa;One-level concentration overhead condenser (23) hot side operation temperature Degree is 50~70 DEG C;Operation gauge pressure is 0.010~0.015MPa;Oxidation feed preheater (21) cold side operation temperature be 50~ 100℃;Operation gauge pressure is 0.6~1.0MPa.
The most according to claim 1, the method for phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, it is special Levy and be that aoxidizing feed preheater (21) uses low low-pressure steam to preheat;One-level concentration overhead condenser (23) cooling water-cooled Solidifying;Concentration tail gas cryoprobe (24) condenses with chilled water.
The most according to claim 1, the method for phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, it is special Levying the reaction condition being oxidation reactor (25): operation temperature is 80~110 DEG C, operation gauge pressure is 0.2~0.4MPa;Isopropyl The mass ratio that benzene (5) charging and compressed air (15) feed is: isopropylbenzene: air=10~20:1;Isopropylbenzene conversion per pass It is 3.2~8.5%.
The most according to claim 1, the method for phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, it is special Levy and be that isopropylbenzene (5) feeding temperature is 80~110 DEG C.
The most according to claim 1, the method for phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, it is special Levying the operating condition being one-level concentration tower (26): operation temperature is 90~170 DEG C, operation gauge pressure is 0.015~0.035MPa.
The most according to claim 1, the method for phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery, it is special Levy the operating condition being concentration tail gas cryoprobe (24): operation temperature is 20~50 DEG C, operation absolute pressure be 0.010~ 0.020MPa。
CN201610520456.XA 2016-07-05 2016-07-05 The method of phenol-acetone device cumyl hydroperoxide upgrading system waste heat recycling Active CN106117018B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610520456.XA CN106117018B (en) 2016-07-05 2016-07-05 The method of phenol-acetone device cumyl hydroperoxide upgrading system waste heat recycling

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610520456.XA CN106117018B (en) 2016-07-05 2016-07-05 The method of phenol-acetone device cumyl hydroperoxide upgrading system waste heat recycling

Publications (2)

Publication Number Publication Date
CN106117018A true CN106117018A (en) 2016-11-16
CN106117018B CN106117018B (en) 2018-12-04

Family

ID=57469321

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610520456.XA Active CN106117018B (en) 2016-07-05 2016-07-05 The method of phenol-acetone device cumyl hydroperoxide upgrading system waste heat recycling

Country Status (1)

Country Link
CN (1) CN106117018B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111606834A (en) * 2020-05-21 2020-09-01 常州瑞华化工工程技术股份有限公司 Concentration method of ethylbenzene hydroperoxide

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN104447214A (en) * 2014-12-01 2015-03-25 中石化上海工程有限公司 Method for reducing energy consumption by employing phenol-acetone device oxidation reaction unit
CN105246867A (en) * 2013-03-14 2016-01-13 凯洛格·布朗及鲁特有限公司 Methods and systems for separating acetone and phenol from one another
CN105237374A (en) * 2015-10-12 2016-01-13 中石化上海工程有限公司 Phenol-acetone device acetone refining system waste heat recovery method

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105246867A (en) * 2013-03-14 2016-01-13 凯洛格·布朗及鲁特有限公司 Methods and systems for separating acetone and phenol from one another
CN104447214A (en) * 2014-12-01 2015-03-25 中石化上海工程有限公司 Method for reducing energy consumption by employing phenol-acetone device oxidation reaction unit
CN105237374A (en) * 2015-10-12 2016-01-13 中石化上海工程有限公司 Phenol-acetone device acetone refining system waste heat recovery method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111606834A (en) * 2020-05-21 2020-09-01 常州瑞华化工工程技术股份有限公司 Concentration method of ethylbenzene hydroperoxide

Also Published As

Publication number Publication date
CN106117018B (en) 2018-12-04

Similar Documents

Publication Publication Date Title
CN104445573A (en) Novel supercritical water oxidation comprehensive treatment system and method
CN205398514U (en) Cyclohexanone refining plant in cyclohexanone production process
CN114408869B (en) Sodium sulfide production system and process for gas-phase fluidization reduction of sodium sulfate
CN107413194A (en) Preparation method and equipment of concentrated ammonia water for desulfurization and denitrification
CN204251405U (en) A kind of Novel supercritical Water oxidize total system
CN105169740A (en) Method for recycling oxidized exhaust gas energy of phenol-acetone device
CN106117018A (en) The method of phenol-acetone device cumyl hydroperoxide upgrading system waste heat recovery
CN111417598A (en) System and method for treating high-salinity high-organic wastewater and recycling energy
CN112409172B (en) Method and system for producing ethyl acetate
CN208943519U (en) The cyclic utilization system of methane steam reforming rear condensate liquid in coke-stove gas
CN105669367B (en) A kind of method for improving cumyl hydroperoxide decomposition yield
CN105985234B (en) Preparation of aromatic dicarboxylic acids
CN111544914A (en) Coal gasification low pressure black water flash distillation heat recovery system
CN204039299U (en) A kind of purifying plant of high-purity sodium formate
CN106278844A (en) A kind of reduce the device and method of consumption of raw materials during propenecarbonyl
CN112694163A (en) Method for quenching waste water of catalytic wet-type acrylonitrile oxidation device
CN108854167A (en) The cyclic utilization system of methane steam reforming rear condensate liquid in coke-stove gas
CN113185411B (en) Method for improving yield and purity of continuously producing di-n-propylamine based on deoxidization technology
CN212673803U (en) A collection device for bipyramid desiccator solvent
CN105237374A (en) Phenol-acetone device acetone refining system waste heat recovery method
CN206188684U (en) Reduce device that propylene carbonylation process central plain material consumed
CN104478775B (en) The method reducing phenol-acetone device oxidation reaction unit energy consumption
CN103030117B (en) Recovering technology for waste acid
CN114057277A (en) Waste alkali wet oxidation system and method
CN217312008U (en) Acrylic acid purification device capable of recycling energy

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant